Package 0904-6671-04
Brand: sildenafil
Generic: sildenafilPackage Facts
Identity
Package NDC
0904-6671-04
Digits Only
0904667104
Product NDC
0904-6671
Description
30 BLISTER PACK in 1 CARTON (0904-6671-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
sildenafil
Generic
sildenafil
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fc0ee2bc-826f-4d18-abb6-49b6795499de", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["a65b5fb3-ca3c-4226-9caa-42fb9a2f7373"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6671-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6671-04", "marketing_start_date": "20121106"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-6671-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6671-06", "marketing_start_date": "20121106"}], "brand_name": "SILDENAFIL", "product_id": "0904-6671_fc0ee2bc-826f-4d18-abb6-49b6795499de", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "0904-6671", "generic_name": "SILDENAFIL", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SILDENAFIL", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA091479", "marketing_category": "ANDA", "marketing_start_date": "20121106", "listing_expiration_date": "20261231"}